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Chronic intestinal pseudo-obstruction with dilated biliary tract as a spectrum of stiff person syndrome in a nondiabetic patient

机译:慢性肠假性梗阻伴胆道扩张是非糖尿病患者的僵硬人综合征谱

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摘要

Stiff person syndrome (SPS) is a rare and challenging neuromuscular junction disorder with typical musculoskeletal manifestations associated with anti-GAD65 antibodies, extra rheumatological manifestations, including neuropsychiatric symptoms and severe dysautonomic troubles. Chronic intestinal pseudo-obstruction (CIPO) is also a rare condition corresponding to a sub-occlusive syndrome, resulting from the functional or structural impairment of smooth neuromuscular tissues of the intestinal tract. In the clinical spectrum of SPS, CIPO has rarely been described and dilated biliary tract has never been described. This present report is therefore the first in the context of anti-GAD65 antibodies with the additional involvement of the biliary tract. Here, we report the case of a 44-year-old woman hospitalized for a rapidly progressive CIPO associated with dilated biliary tract, revealing a typical SPS with slowly progressive rheumatologic complaints relegated to the background. The concomitant improvement of the neuromuscular function on skeletal, intestinal and biliary tree systems with the good outcomes of anti-GAD65 titer under immunosuppressant drugs, allowed us to link all three organic involvements to the antibody pathogenicity on the respective neuromuscular junctions. Therefore, we discussed their common pathogeny based on our patient’s treatment outcome.
机译:僵人综合症(SPS)是一种罕见且具有挑战性的神经肌肉交界障碍,具有与抗GAD65抗体相关的典型肌肉骨骼表现,额外的风湿病表现,包括神经精神症状和严重的自主神经障碍。慢性肠假性梗阻(CIPO)也是一种罕见的疾病,对应于闭塞性综合征,这是由于肠道平滑神经肌肉组织的功能或结构受损所致。在SPS的临床范围内,很少描述CIPO,从未描述过胆道扩张。因此,本报告是抗GAD65抗体与胆道的额外牵连的第一个报告。在此,我们报道了一名因胆道扩张而迅速进展的CIPO住院的44岁女性的病例,揭示了典型的SPS并伴有逐渐进展的风湿病主诉。骨骼,肠道和胆管树系统神经肌肉功能的伴随改善,以及在免疫抑制剂作用下抗GAD65滴度的良好结果,使我们能够将所有三种有机物与各自神经肌肉接头上的抗体致病性联系起来。因此,我们根据患者的治疗结果讨论了它们的常见病原体。

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